Mapping Gene Associations in Human Mitochondria using Clinical Disease Phenotypes

Nuclear genes encode most mitochondrial proteins, and their mutations cause diverse and debilitating clinical disorders. To date, 1,200 of these mitochondrial genes have been recorded, while no standardized catalog exists of the associated clinical phenotypes. Such a catalog would be useful to devel...

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Detalles Bibliográficos
Autores principales: Scharfe, Curt, Lu, Henry Horng-Shing, Neuenburg, Jutta K., Allen, Edward A., Li, Guan-Cheng, Klopstock, Thomas, Cowan, Tina M., Enns, Gregory M., Davis, Ronald W.
Formato: Texto
Lenguaje:English
Publicado: Public Library of Science 2009
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2668170/
https://www.ncbi.nlm.nih.gov/pubmed/19390613
http://dx.doi.org/10.1371/journal.pcbi.1000374

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2668170/
https://www.ncbi.nlm.nih.gov/pubmed/19390613
http://dx.doi.org/10.1371/journal.pcbi.1000374

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